Work on a range of clinical studies for small to large pharmaceutical and biotech clients while feeling valued and supported in your day-to-day work.

We are seeking a hands on Programmer with attention to detail and strong work ethic to work as part of the statistical and programming team providing programming support as outlined below to a variety of clients in the Veramed portfolio. This role provides the opportunity to progress towards becoming a Lead Programmer at Veramed.

KEY RESPONSIBILITIES:

This role entails a wide variety of responsibilities and client exposure – you are certainly not pigeon holed.

Below is a range of the types of tasks you could be carrying out on a daily basis. As with many roles at Veramed, you have the opportunity to shape their direction dependent on client needs and your own career aspirations.

PROGRAMMING:

• Program and QC datasets and TFLs following specifications and good programming practice.
• Develop dataset specifications that conform to CDISC data standards.
• Attend and contribute to internal and client study team meetings.
• Mentor less experienced members of the team.

OPPORTUNITIES FOR: 

• Development into lead programmer or technical role.
• Gaining experience across different therapeutic areas and phases.
• Presenting at conferences.
• Peer mentoring and/or line management.
• Developing innovative solutions to aid study reporting.
• Contributing to initiatives that consider employees, the environment and our local communities as part of our B Corp accreditation.

WHAT TO EXPECT:

• A warm, friendly working environment in which to thrive both personally and professionally.
• A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
• Exposure to a wide range of clients and projects, allowing you to diversify your workload and work closely with some of the biggest pharma companies in the industry.
• Work with a truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry.
• The ability to truly own your role and develop your skills and experience.

BENEFICIAL EXPERIENCE:

• Understanding of the clinical drug development process and relevant disease areas.
• Awareness of industry and project standards as well as ICH guidelines.
• Proficiency in using SAS or other statistical software (e.g. R) appropriate to the level of seniority.
• A good understanding of CDISC data standards.
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
• Ability to work independently and as part of a team.

If you have a passion for contributing to high quality deliverables, thrive when working closely with team members of all levels of experience and want to work for a company where you truly feel you can add value, this role could be for you. Apply now.